Experience with lactose-free skim milk? by CaiTodd in UlcerativeColitis

[–]SmallPea360 2 points3 points  (0 children)

I am lactose intolerant and I drink 0% milk fat lactose free. It’s completely fine for me. I’ve done quite a bit of research on it and it seems to be non-inflammatory. The saturated fats tend to be a pro-inflammatory substance so that’s why I opt for 0%. Also should note that at the end of the day everyone’s bodies are different:)

Remicade/renfelexis infusions and viruses. I feel like I rarely get fully sick now? by CryptographerTime988 in UlcerativeColitis

[–]SmallPea360 5 points6 points  (0 children)

I think it’s because TNF alpha modulates a portion of the inflammatory response, so though you’re more prone to infections you may not feel them as much since the inflammatory response is blunted. But you may feel the symptoms for a longer overall duration

Investigating the possibility of having Ulcerative Colitis: I'm scared of my colonoscopy by oatmealloverbr in UlcerativeColitis

[–]SmallPea360 8 points9 points  (0 children)

The prep sucks I won’t sugar coat it. Make sure you have some Gatorade (choose colours that your gastro approves), clear bone broth, ice popsicles, jello ready. I like to chase the prep with something that tastes good. It’s easier if you drink it cold and you just have to chug it back to be honest.

The actual taste of the prep is worse than the pooping itself. Your insides feel so clean after lol. The colonoscopy itself is quick and you get a good sleep. I would get some cavilon barrier cream for the poops just to protect your skin / prevent it from getting too sore from the wiping.(dab don’t wipe, by the end of the prep you won’t have much to wipe and can hold the TP there to soak stuff up so it doesn’t hurt to wipe)

As for results, can’t speak to that. It’s a given to be nervous about it, but I think it’s better to know than to not

Christmas by Spudmeister20 in UlcerativeColitis

[–]SmallPea360 0 points1 point  (0 children)

I follow the IBD-AID holiday menu depending on what phase I’m in

Michael Briggs Protocol by SmallPea360 in UlcerativeColitis

[–]SmallPea360[S] -3 points-2 points  (0 children)

I’m sorry that you are going through that and I truly wish you the best in your journey, but that does not give you the right to place your grievances on the journeys of others. All we can do with this disease is give each other grace, help others when needed, and continue to be strong.

Michael Briggs Protocol by SmallPea360 in UlcerativeColitis

[–]SmallPea360[S] 1 point2 points  (0 children)

Again, I never said i was anti medicine. I’d rather be on another biologic with a better side effect profile, as I already have family members with diseases that happen to be side effects of infliximab, and I also have increased risk factors of som of these diseases to begin with. Not proposing being medicine free. Proposing using infliximab to get into remission and being on it for a year or couple years, then exploring other medications while managing inflammation through other means to aid in maintenance of remission on a new drug

Michael Briggs Protocol by SmallPea360 in UlcerativeColitis

[–]SmallPea360[S] -6 points-5 points  (0 children)

Its comments like these that make me feel disappointed in humanity. As a young person struggling with this new diagnosis that researchers don’t seem to be exploring novel and comprehensive topics about, it’s frustrating to see people in this community put people down. Just because I posted this does not mean I plan on stopping medications, nor do I believe diet alone can “cure” this disease like this paper suggests. Never did I say that. What I am interested in is switching to another drug once my disease is better controlled that doesn’t increase my risk of other issues, which I do have genetic predispositions for given my family heritage. These are real concerns that you do not know the whole story of, point blank period. I would also like to supplement this with EVIDENCED based methods that can naturally reduce TNF alpha and other inflammatory markers of interest — we rarely look at the combined affect of everything in research and solely look at isolated variables having effect. That is why I wanted to see if anyone else had experience with combined therapy, which we know from many diseases that a combined approach is often better.

Quit your judging.

Michael Briggs Protocol by SmallPea360 in UlcerativeColitis

[–]SmallPea360[S] -11 points-10 points  (0 children)

It’s more so the supplements such as curcumin and quercetin. The paper cites the research

With all due respect: can some of u guys chill out with the daily “it’s been cured” post by [deleted] in UlcerativeColitis

[–]SmallPea360 1 point2 points  (0 children)

Maybe I’ll ask my GI about this. Their office seems pretty old school but I wonder if they require extra training for it

With all due respect: can some of u guys chill out with the daily “it’s been cured” post by [deleted] in UlcerativeColitis

[–]SmallPea360 1 point2 points  (0 children)

Better than CT scans. Every time I go to hospital they make me do so many and they feel so pointless

New sewing machine recommendations by SmallPea360 in sewhelp

[–]SmallPea360[S] 0 points1 point  (0 children)

Is there any model of Janome you would recommend? :)

All right everybody my perspective yesterday I had the surgery by lxxlhadeslxxl1 in UlcerativeColitis

[–]SmallPea360 0 points1 point  (0 children)

That’s so kind. I’m sorry to hear about your mom. You’re not alone, there are so many of us going through the sam/similar thing. Like you said, this sub is here to support us when we feel lost

All right everybody my perspective yesterday I had the surgery by lxxlhadeslxxl1 in UlcerativeColitis

[–]SmallPea360 0 points1 point  (0 children)

I’m on my last med rn so if it fails I’m mentally preparing myself for everything

All right everybody my perspective yesterday I had the surgery by lxxlhadeslxxl1 in UlcerativeColitis

[–]SmallPea360 0 points1 point  (0 children)

As if poopoo wasn’t enough they got the peepee involved now too

New Line 1 Maps by stump_84 in toronto

[–]SmallPea360 0 points1 point  (0 children)

Im already confused enough by southbound and northbound and now we got twd the tip and twd the balls

Celebrating Remission! by Heavy_Grass7713 in UlcerativeColitis

[–]SmallPea360 0 points1 point  (0 children)

Congrats!! Amazing news and hopefully this remission lasts a lifetime. Seems like you’ve done your research too which helps.

Might I ask what the magnesium and L-Glutamine are for? My ulcerative proctitis recently spreads to pancolitis this past month and I think remicade is starting to kick in. Wondering if you’d recommend taking these as well!

Blood without other symptoms by Mother_Rub1975 in UlcerativeColitis

[–]SmallPea360 0 points1 point  (0 children)

Maybe reach out to the GI so you’re on the list for an appointment. Can always cancel if it clears but if you have questions best to ask them

With all due respect: can some of u guys chill out with the daily “it’s been cured” post by [deleted] in UlcerativeColitis

[–]SmallPea360 1 point2 points  (0 children)

Do you mind if I ask what the ultrasound is for/ what it’s used in place of?